. . . . . . . . . . . . "[The variant CBS c.844_855ins68 -- that is, the allele carrying the insertion (`ins` or `i`) as opposed to the wild-type allele designated as deletion (`del` or `d`) -- was significantly overrepresented in meningioma patients (dd/ id/ii: 0.81/0.18/0.01) in comparison with the controls (dd/id/ii: 0.88/0.12/0; 2 df, chi-square 8.97, p = 0.011; multiple nominal regression with age and sex as covariables).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2014-02-25"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2014-10-02T12:39:42+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .